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"71921-182-50" National Drug Code (NDC)

Ibuprofen 500 TABLET, FILM COATED in 1 BOTTLE (71921-182-50)
(Florida Pharmaceutical Products, LLC)

NDC Code71921-182-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (71921-182-50)
Product NDC71921-182
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIbuprofen
Non-Proprietary NameIbuprofen
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211021
Marketing Category NameANDA
Application NumberANDA071268
ManufacturerFlorida Pharmaceutical Products, LLC
Substance NameIBUPROFEN
Strength800
Strength Unitmg/1
Pharmacy ClassesAnti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71921-182-50





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